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Case Report

Three Cases of the Moya Moya Disease

The Ewha Medical Journal 1986;9(2):135-142. Published online: July 24, 2015

Department of Neurosurgery, College of Medicine, Ewha Womans University, Korea.

Corresponding author: Kyu Man Shin. Department of Neuropsugery, College of Medicine, Ewha Womans University, Korea.

Copyright © 1986. Ewha Womans University School of Medicine

This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

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  • Moya Moya disease is a rare chronic occlusive cerebrovascular disease of unknown etiology for which no effective treatment has been found. This disease has distinct angiographic features. These include 1) Either marked stenosis or complete occlusion of the distal internal carotid arteries. 2) Poorly visualized anterior and middle cerebral arteries at their proximal portions. 3) Well developed fine vascular networks at the base of the brain. These features are peculiar findings of this disease and the clue of the occlusion and its collateral circulation. Authors reported 3 cases of moya moya disease is discussed.

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